Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1165364Erstellt: 27. Oktober 2026

2-Cyanoethyl tetraisopropylphosphorodiamidite → N-biotinyl-aminopropyl 2-cyanoethyl N,N-diisopropylphosphoramidite

https://huagongshe.com/reaction/1165364

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Cyanoethyl tetraisopropylphosphorodiamiditeHCID 128153—
EduktSodium BicarbonateHCID 516892—
EduktN-biotinylaminopropanolHCID 131716340—
EduktHCID 178458033HCID 178458033—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-biotinyl-aminopropyl 2-cyanoethyl N,N-diisopropylphosphoramiditeHCID 15085419—

Reaktionsschritte

To a solution of 150 mg of N-biotinylaminopropanol (2b) in 5 ml of dry DMF was added 65 mg of diisopropylammonium tetrazolide and 0.300 ml of 2-cyanoethyl N,N,N',N'-tetraisopropylphosphorodiamidite. The resulting solution was stirred at room temperature for 1.0 hr and then poured onto 50 ml of 5% aqueous sodium bicarbonate. The mixture was extracted with two 50 ml portions of methylene chloride, and the combined extracts were washed with 5% sodium bicarbonate and brine, dried over sodium sulfate, and evaporated to afford the crude product as a thick oil. This was dissolved in 2 ml of dry methylene chloride affording a solution that was added dropwise to 30 ml of rapidly stirring petroleum ether. The colorless precipitate which formed was collected by suction filtration under argon, affording after drying at room temperature under vacuum 151 mg (60%) of a colorless solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04908453
Quelldatensatzuspto-grants-1990_03
ORD IDord-7164f27389e64b539be65359be962472
Quellennotizuspto-grants-1990_03